510(k) Report

510(k) · Cleared

Cleared

IPS Style Ceram, IPS Style Ceram One, IPS Style Press

K152103510(k) TraditionalCleared May 20, 2016296-day reviewClass II21 CFR 872.6660

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Ivoclar Vivadent, AG · EIH Powder, Porcelain

Cleared on May 20, 2016 as substantially equivalent to K121359 (Ivoclar Vivadent, AG, 2012) and 1 other predicate after a 296-day review. Its family tree reaches back 3 generations to 1994.

Decided
May 20, 2016
Review
296 days
Class
Class II
Product code
EIH
Recalls
None
Predicates
2

Its longest line of descent runs back 3 generations to K940252 (1994). 4 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 2012: 1 other ancestorK940252 · Finesse Porcelain System · Dentsply Intl. · 1994K041335 · PTM System · Dentsply International · 2004K071848 · Ips Inline Pom System · Ivoclar Vivadent, Inc. · 2007199019952000200520102015
  1. Root · 3 generations backK940252 Finesse Porcelain SystemDentsply Intl. · 1994
  2. 2 generations backK041335 PTM SystemDentsply International · 2004
  3. 1 generation backK071848 Ips Inline Pom SystemIvoclar Vivadent, Inc. · 2007
  4. This deviceK152103 IPS Style Ceram, IPS Style Ceram One, IPS Style PressIvoclar Vivadent, AG · 2016
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K940252Finesse Porcelain SystemDentsply Intl.1994—
−2K041335PTM SystemDentsply International2004—
−1K071848Ips Inline Pom SystemIvoclar Vivadent, Inc.2007—
0 (this device)K152103IPS Style Ceram, IPS Style Ceram One, IPS Style PressIvoclar Vivadent, AG2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201210
FIG. 1 — Lineage of K152103, 1994–2016Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in EIH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new EIH device

  1. #1 K192231 Dental Glass Ceramics Blocksscore 15.3 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K121359Ips 99 One and Ips 99 Ceram
Summary page 4
…CFR Regulation (872.6660) (Classification Code EIH) Predicate Device: IPS 99 One and IPS 99 Ceram (K121359) IPS InLine PoM System (K071848) Device Description: IPS Style comprises both materials for the c…
Ivoclar Vivadent, AG2012—
*K071848Ips Inline Pom System
Summary page 4
…(Classification Code EIH) Predicate Device: IPS 99 One and IPS 99 Ceram (K121359) IPS InLine PoM System (K071848) Device Description: IPS Style comprises both materials for the conventional veneering technique and the press technique. •…
Ivoclar Vivadent, Inc.2007—

Also cleared against K121359: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 22 years and passes through 4 companies; a new generation was cleared every 8.7 years on median.
  • None of the 4 ancestors has a recall.
  • 2 other devices also cite its predicate K121359.

How does its category compare?

All EIH devices

EIH Powder, Porcelain: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · EIH

13in 2025

2007: 152008: 152009: 152010: 142011: 142012: 92013: 162014: 182015: 232016: 222017: 162018: 102019: 162020: 132021: 172022: 162023: 152024: 282025: 132026 (partial year): 14
2007high 28 (2024) · low 9 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EIH

84in 2025

2007: 63 days median2008: 87 days median2009: 79 days median2010: 89 days median2011: 80 days median2012: 96 days median2013: 107 days median2014: 118 days median2015: 118 days median2016: 187 days median2017: 149 days median2018: 139 days median2019: 125 days median2020: 155 days median2021: 131 days median2022: 89 days median2023: 114 days median2024: 89 days median2025: 84 days median2026 (partial year): 73 days median
2007high 187 (2016) · low 63 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · EIH

1in 2025

2016: 212025: 1
2007high 21 (2016) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · EIH

1in 2025

2008: 12011: 12013: 62014: 12016: 42017: 12018: 22019: 12021: 222024: 72025: 1
2007high 22 (2021) · low 0 (2007)2025

MAUDE reports naming product code EIH, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007156300
2008158701
2009157900
2010148900
2011148001
201299600
20131610706
20141811801
20152311800
201622187214
20171614901
20181013902
20191612501
20201315500
202117131022
2022168900
20231511400
2024288907
2025138411
202614730—

What is it indicated for?

Intended Use: 1PS Style Press — Pressing on metal frameworks and superstructures for the fabrication of full-contour crowns and bridges (staining technique) — Pressing on metal frameworks and superstructures for the fabrication of partially anatomic crowns and bridges (cut-back technique) ~ Pressing of ceramic margins (metal-ceramic) - Pressing of gingiva components (metal-ceramic) - Processing on the most popular dental alloys in the CTE range of 13.8 —…

Read the full statement (208 words)

Intended Use: 1PS Style Press

— Pressing on metal frameworks and superstructures for the fabrication of full-contour crowns and bridges (staining technique)

— Pressing on metal frameworks and superstructures for the fabrication of partially anatomic crowns and bridges (cut-back technique)

~ Pressing of ceramic margins (metal-ceramic)

- Pressing of gingiva components (metal-ceramic)

- Processing on the most popular dental alloys in the CTE range of 13.8 — 14.5 10-6/K

(25 - 500°C) (Cu< 1%, Ag < 10%)

- Veneering with the layering materials of IPS Style in the conventional layering technique

— Characterization with IPS Ivocolor Shade and Essence stains

— Glazing with IPS Ivocolor Glaze

Intended Use: IPS Style Ceram and IPS Style Ceram Onc

— Conventional multi-layer veneering ceramic for the most popular dental alloys

(including electroplating) in the CTE range of 13.8 — 15.2 x 10-6/K (25 — 500°C)

(IPS Style Ceram)

— One-layer veneering ceramic for the most popular dental alloys (including electroplating)

in the CTE range of 13.8 — 15.2 x 10-6/K (25 ~ 500°C) (IPS Style Ceram One)

— Veneers on refractory die material (only IPS Style Ceram)

— Characterization and veneering of IPS Style Press restorations

— Characterization with IPS Ivocolor Shade and Essence stains

- Glazing with IPS Ivocolor Glaze

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K152103: IPS Style Ceram, IPS Style Ceram One, IPS Style Press.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K152103

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026